bladder cancer tissue microarrays tma Search Results


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OriGene multicancer tissue cdna array
Figure 1 BVES expression is significantly downregulated, and it is mislocalized in human colon carcinoma. (A) A human BVES hydrolysis probe was used to perform qPCR on an Origene <t>cDNA</t> array (TissueScan Cancer Survey I). Ct values were normalized to β-actin and then presented as fold reduction from matched normal (N) (n = 3 per tissue type) and tumor (T) tissue (n = 9 per tissue type). ***P < 0.001, 2-tailed unpaired t test. (B) Analysis of the combined Moffit Cancer Center and Vanderbilt Medical Center colon tumor expression array data set (10, normal samples; 6, adenomas; 33, stage I; 76, stage 2; 82, stage 3; and 59, stage 4; for combined total of 250 CRC samples). For whisker plots, the bottom and top of the boxes are the 25th and 75th percentile, respectively (the lower and upper quartiles, respectively), and the band near the middle of the box is the 50th percentile (median). The whiskers extend to the most extreme data points, which are no more than 1.5 times the interquartile range from the box. *P = 0.04, ***P = 0.001, ****P = 0.0001. (C) Representative immunofluorescence images from normal colon or adenocarci- noma (original magnification, ×400) of H&E, BVES (green), ZO-1 (red), DAPI (blue), and merged images.
Multicancer Tissue Cdna Array, supplied by OriGene, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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OriGene cdna array
( A ) Validation of relative SETD6 expression in different bladder cells was carried out using qPCR. p ≤ 0.05 were considered to be statistically significant (*). The samples were measured in triplicates and the experiment was repeated 3 times. ( B ) <t>cDNA</t> <t>array</t> was performed with bladder cancer tissues ( n = 24) representing different stages and SETD6 expression was analyzed by qPCR. ( C ) Basal level of SETD6 protein was detected using anti-SETD6 antibody by western blotting. ( D ) Immunocytochemistry in different bladder cancer cell lines cells showing cytoplasmic and nuclear SETD6. ( E ) SETD6 protein was detected using anti-SETD6 antibody by western blot in bladder cancer tissues ( n = 9) compared to non-cancerous bladder tissues.
Cdna Array, supplied by OriGene, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology glioma invasion tissue microarray tma
( A ) Validation of relative SETD6 expression in different bladder cells was carried out using qPCR. p ≤ 0.05 were considered to be statistically significant (*). The samples were measured in triplicates and the experiment was repeated 3 times. ( B ) <t>cDNA</t> <t>array</t> was performed with bladder cancer tissues ( n = 24) representing different stages and SETD6 expression was analyzed by qPCR. ( C ) Basal level of SETD6 protein was detected using anti-SETD6 antibody by western blotting. ( D ) Immunocytochemistry in different bladder cancer cell lines cells showing cytoplasmic and nuclear SETD6. ( E ) SETD6 protein was detected using anti-SETD6 antibody by western blot in bladder cancer tissues ( n = 9) compared to non-cancerous bladder tissues.
Glioma Invasion Tissue Microarray Tma, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Novus Biologicals paraffin embedded breast cancer tissue arrays
( A ) Validation of relative SETD6 expression in different bladder cells was carried out using qPCR. p ≤ 0.05 were considered to be statistically significant (*). The samples were measured in triplicates and the experiment was repeated 3 times. ( B ) <t>cDNA</t> <t>array</t> was performed with bladder cancer tissues ( n = 24) representing different stages and SETD6 expression was analyzed by qPCR. ( C ) Basal level of SETD6 protein was detected using anti-SETD6 antibody by western blotting. ( D ) Immunocytochemistry in different bladder cancer cell lines cells showing cytoplasmic and nuclear SETD6. ( E ) SETD6 protein was detected using anti-SETD6 antibody by western blot in bladder cancer tissues ( n = 9) compared to non-cancerous bladder tissues.
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BioChain Institute colon cancer tissues microarray
( A ) Validation of relative SETD6 expression in different bladder cells was carried out using qPCR. p ≤ 0.05 were considered to be statistically significant (*). The samples were measured in triplicates and the experiment was repeated 3 times. ( B ) <t>cDNA</t> <t>array</t> was performed with bladder cancer tissues ( n = 24) representing different stages and SETD6 expression was analyzed by qPCR. ( C ) Basal level of SETD6 protein was detected using anti-SETD6 antibody by western blotting. ( D ) Immunocytochemistry in different bladder cancer cell lines cells showing cytoplasmic and nuclear SETD6. ( E ) SETD6 protein was detected using anti-SETD6 antibody by western blot in bladder cancer tissues ( n = 9) compared to non-cancerous bladder tissues.
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SuperBioChips colorectal cancer tissue microarrays
( A ) Validation of relative SETD6 expression in different bladder cells was carried out using qPCR. p ≤ 0.05 were considered to be statistically significant (*). The samples were measured in triplicates and the experiment was repeated 3 times. ( B ) <t>cDNA</t> <t>array</t> was performed with bladder cancer tissues ( n = 24) representing different stages and SETD6 expression was analyzed by qPCR. ( C ) Basal level of SETD6 protein was detected using anti-SETD6 antibody by western blotting. ( D ) Immunocytochemistry in different bladder cancer cell lines cells showing cytoplasmic and nuclear SETD6. ( E ) SETD6 protein was detected using anti-SETD6 antibody by western blot in bladder cancer tissues ( n = 9) compared to non-cancerous bladder tissues.
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Image Search Results


Figure 1 BVES expression is significantly downregulated, and it is mislocalized in human colon carcinoma. (A) A human BVES hydrolysis probe was used to perform qPCR on an Origene cDNA array (TissueScan Cancer Survey I). Ct values were normalized to β-actin and then presented as fold reduction from matched normal (N) (n = 3 per tissue type) and tumor (T) tissue (n = 9 per tissue type). ***P < 0.001, 2-tailed unpaired t test. (B) Analysis of the combined Moffit Cancer Center and Vanderbilt Medical Center colon tumor expression array data set (10, normal samples; 6, adenomas; 33, stage I; 76, stage 2; 82, stage 3; and 59, stage 4; for combined total of 250 CRC samples). For whisker plots, the bottom and top of the boxes are the 25th and 75th percentile, respectively (the lower and upper quartiles, respectively), and the band near the middle of the box is the 50th percentile (median). The whiskers extend to the most extreme data points, which are no more than 1.5 times the interquartile range from the box. *P = 0.04, ***P = 0.001, ****P = 0.0001. (C) Representative immunofluorescence images from normal colon or adenocarci- noma (original magnification, ×400) of H&E, BVES (green), ZO-1 (red), DAPI (blue), and merged images.

Journal: Journal of Clinical Investigation

Article Title: BVES regulates EMT in human corneal and colon cancer cells and is silenced via promoter methylation in human colorectal carcinoma

doi: 10.1172/jci44228

Figure Lengend Snippet: Figure 1 BVES expression is significantly downregulated, and it is mislocalized in human colon carcinoma. (A) A human BVES hydrolysis probe was used to perform qPCR on an Origene cDNA array (TissueScan Cancer Survey I). Ct values were normalized to β-actin and then presented as fold reduction from matched normal (N) (n = 3 per tissue type) and tumor (T) tissue (n = 9 per tissue type). ***P < 0.001, 2-tailed unpaired t test. (B) Analysis of the combined Moffit Cancer Center and Vanderbilt Medical Center colon tumor expression array data set (10, normal samples; 6, adenomas; 33, stage I; 76, stage 2; 82, stage 3; and 59, stage 4; for combined total of 250 CRC samples). For whisker plots, the bottom and top of the boxes are the 25th and 75th percentile, respectively (the lower and upper quartiles, respectively), and the band near the middle of the box is the 50th percentile (median). The whiskers extend to the most extreme data points, which are no more than 1.5 times the interquartile range from the box. *P = 0.04, ***P = 0.001, ****P = 0.0001. (C) Representative immunofluorescence images from normal colon or adenocarci- noma (original magnification, ×400) of H&E, BVES (green), ZO-1 (red), DAPI (blue), and merged images.

Article Snippet: BVES TaqMan qRT-PCR was performed on a multicancer tissue cDNA array (TissueScan Cancer Survey I, OriGene) according to the manufacturers protocol.

Techniques: Expressing, Whisker Assay, Immunofluorescence

( A ) Validation of relative SETD6 expression in different bladder cells was carried out using qPCR. p ≤ 0.05 were considered to be statistically significant (*). The samples were measured in triplicates and the experiment was repeated 3 times. ( B ) cDNA array was performed with bladder cancer tissues ( n = 24) representing different stages and SETD6 expression was analyzed by qPCR. ( C ) Basal level of SETD6 protein was detected using anti-SETD6 antibody by western blotting. ( D ) Immunocytochemistry in different bladder cancer cell lines cells showing cytoplasmic and nuclear SETD6. ( E ) SETD6 protein was detected using anti-SETD6 antibody by western blot in bladder cancer tissues ( n = 9) compared to non-cancerous bladder tissues.

Journal: Oncotarget

Article Title: SETD6 regulates NF-κB signaling in urothelial cell survival: Implications for bladder cancer

doi: 10.18632/oncotarget.14750

Figure Lengend Snippet: ( A ) Validation of relative SETD6 expression in different bladder cells was carried out using qPCR. p ≤ 0.05 were considered to be statistically significant (*). The samples were measured in triplicates and the experiment was repeated 3 times. ( B ) cDNA array was performed with bladder cancer tissues ( n = 24) representing different stages and SETD6 expression was analyzed by qPCR. ( C ) Basal level of SETD6 protein was detected using anti-SETD6 antibody by western blotting. ( D ) Immunocytochemistry in different bladder cancer cell lines cells showing cytoplasmic and nuclear SETD6. ( E ) SETD6 protein was detected using anti-SETD6 antibody by western blot in bladder cancer tissues ( n = 9) compared to non-cancerous bladder tissues.

Article Snippet: cDNA array (Origene, TissueScanTM Cancer and Normal Tissue cDNA Arrays) was used to determine the level of SETD6 expression in different bladder tissue samples ( n = 24).

Techniques: Biomarker Discovery, Expressing, Western Blot, Immunocytochemistry